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Proteasome inhibitors prevent cell death and prolong survival of mice challenged by Shiga toxin

Shiga toxin (Stx) causes fatal systemic complications. Stx induces apoptosis, but the mechanism of which is unclear. We report that Stx induced rapid reduction of short-lived anti-apoptotic proteins followed by activation of caspase 9 and the progression of apoptosis. Proteasome inhibitors prevented...

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Autores principales: Hattori, Takayuki, Watanabe-Takahashi, Miho, Ohoka, Nobumichi, Hamabata, Takashi, Furukawa, Koichi, Nishikawa, Kiyotaka, Naito, Mikihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534485/
https://www.ncbi.nlm.nih.gov/pubmed/26273560
http://dx.doi.org/10.1016/j.fob.2015.06.005
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author Hattori, Takayuki
Watanabe-Takahashi, Miho
Ohoka, Nobumichi
Hamabata, Takashi
Furukawa, Koichi
Nishikawa, Kiyotaka
Naito, Mikihiko
author_facet Hattori, Takayuki
Watanabe-Takahashi, Miho
Ohoka, Nobumichi
Hamabata, Takashi
Furukawa, Koichi
Nishikawa, Kiyotaka
Naito, Mikihiko
author_sort Hattori, Takayuki
collection PubMed
description Shiga toxin (Stx) causes fatal systemic complications. Stx induces apoptosis, but the mechanism of which is unclear. We report that Stx induced rapid reduction of short-lived anti-apoptotic proteins followed by activation of caspase 9 and the progression of apoptosis. Proteasome inhibitors prevented the reduction of anti-apoptotic proteins, and inhibited caspase activation and apoptosis, suggesting that the reduction of anti-apoptotic proteins is a prerequisite for Stx-induced apoptosis. A clinically approved proteasome inhibitor, bortezomib, prolonged the survival of mice challenged by Stx. These results imply that proteasome inhibition may be a novel approach to prevent the fatal effects of Stx.
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spelling pubmed-45344852015-08-13 Proteasome inhibitors prevent cell death and prolong survival of mice challenged by Shiga toxin Hattori, Takayuki Watanabe-Takahashi, Miho Ohoka, Nobumichi Hamabata, Takashi Furukawa, Koichi Nishikawa, Kiyotaka Naito, Mikihiko FEBS Open Bio Research article Shiga toxin (Stx) causes fatal systemic complications. Stx induces apoptosis, but the mechanism of which is unclear. We report that Stx induced rapid reduction of short-lived anti-apoptotic proteins followed by activation of caspase 9 and the progression of apoptosis. Proteasome inhibitors prevented the reduction of anti-apoptotic proteins, and inhibited caspase activation and apoptosis, suggesting that the reduction of anti-apoptotic proteins is a prerequisite for Stx-induced apoptosis. A clinically approved proteasome inhibitor, bortezomib, prolonged the survival of mice challenged by Stx. These results imply that proteasome inhibition may be a novel approach to prevent the fatal effects of Stx. Elsevier 2015-06-12 /pmc/articles/PMC4534485/ /pubmed/26273560 http://dx.doi.org/10.1016/j.fob.2015.06.005 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research article
Hattori, Takayuki
Watanabe-Takahashi, Miho
Ohoka, Nobumichi
Hamabata, Takashi
Furukawa, Koichi
Nishikawa, Kiyotaka
Naito, Mikihiko
Proteasome inhibitors prevent cell death and prolong survival of mice challenged by Shiga toxin
title Proteasome inhibitors prevent cell death and prolong survival of mice challenged by Shiga toxin
title_full Proteasome inhibitors prevent cell death and prolong survival of mice challenged by Shiga toxin
title_fullStr Proteasome inhibitors prevent cell death and prolong survival of mice challenged by Shiga toxin
title_full_unstemmed Proteasome inhibitors prevent cell death and prolong survival of mice challenged by Shiga toxin
title_short Proteasome inhibitors prevent cell death and prolong survival of mice challenged by Shiga toxin
title_sort proteasome inhibitors prevent cell death and prolong survival of mice challenged by shiga toxin
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534485/
https://www.ncbi.nlm.nih.gov/pubmed/26273560
http://dx.doi.org/10.1016/j.fob.2015.06.005
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